US5304569A - Compositions and their use in lowering intraocular pressure - Google Patents

Abstract

Compounds of formula: ##STR1## where X is --CH₂ --, --CH(CH₃)--, --CHR₃ --CH₂ -- or --CR₃ ═CH-- and R₁, R₂ and R₃, which can be the same or different, are each H or CH₃ or a stereoisomer or pharmaceutically acceptable salt thereof, and pharmaceutical compositions containing them, are useful for lowering intraocular pressure in a mammal, e.g. in the treatment of glaucoma.

Description

The present invention relates to the use of certain 4-substituted imidazoles in lowering intraocular pressure, e.g. in the treatment of glaucoma.

Glaucoma is a group of diseases characterized by an increase in intraocular pressure which causes pathological changes in the optic disk and typical defects in the field of vision. Known antiglaucoma drugs are, e.g., timolol and apraclonidine (p-aminoclonidine).

It has now been observed that imidazole derivatives of the formula: ##STR2## where X is --CH₂ --, --CH(CH₃)--, --CHR₃ --CH₂ -- or --CR₃ ═CH-- and R₁, R₂ and R₃, which can be the same or different, are each H or CH₃, and their salts and stereoisomers are effective in lowering intraocular pressure.

The compounds of formula (I) are known, e.g. from European Patent Publication Nose. 24829, 34473, 34474 and 72615. In these publications the compounds have been described as antihypertensive agents.

The antiglaucoma activity of the compounds of formula (I) was determined by measuring the decrease of intraocular pressure (IOP) in rabbits. The tests were carried out as follows:

Adult rabbits of both sexes (weight 3-4 kg) were used in all studies. IOP was measure by tonometry using a Digilab Modular One Pneuma Tonometry following induction of a corneal anesthesia with a drop of 0.4% oxybuprocain (Oftan Obucain®, Star, Finland). Baseline IOP was determined for both eyes at 120, 60 , 30 minutes and just before topical application of the studied compounds or vehicle (control animals) on either left or right eye. The compounds were administered dissolved or suspended in a phosphate buffer, pH 6.5, at the concentration indicated in Table 1. After application IOP was determined for both eyes at 30, 60, 120, 180, 240 and 300 minutes.

The results obtained are presented in Table 1, where the maximal IOP decrease (mmHg) in response to each compound is shown. Para-aminoclonidine and timolol were studied as positive references.

The following compounds of formula (I) were tested:

______________________________________                                    
NO.     NAME                                                              
______________________________________                                    
1.      4-(2,6-dimethylbenzyl)-1H-imidazole                               
2.      4-[2-(2,6-dimethylphenyl)ethyl]-1H-imidazole                      
3.      4-[2-(2,6-dimethylphenyl)ethenyl]-1H-imidazole                    
4.      4-[2-(2,6-dimethylphenyl)-1-methylethyl]-1H-                      
        imidazole                                                         
5.      4-[2-(2,6-dimethylphenyl)-1-methylethenyl]-1H-                    
        imidazole                                                         
6.      4-[(α-methyl)-2-methylbenzyl]-1H-imidazole                  
7.      4-[(α-methyl)-2,3-dimethylbenzyl]-1H-imidazole,             
        dextro isomer                                                     
8.      4-[(α-methyl)-2,3-dimethylbenzyl]-1H-imidazole.             
______________________________________                                    

              TABLE 1                                                     
______________________________________                                    
Maximal decrease in intra-                                                
ocular pressure, mmHg Concentration and                                   
Compound           Contralateral                                          
                              volume of drug                              
No.     Treated eye                                                       
                   eye        solution dropped                            
______________________________________                                    
Controls                                                                  
        +1.2       -0.5       0    (50 μl)                             
1.      -2.1       -1.4       1    mg/ml (25 μl)                       
2.      -1.4       -1.4       5    mg/ml (50 μl)                       
3.      -0.6       -2.8       12.5 mg/ml (100 μl)                      
4.      -1.9       -2.1       2.5  mg/ml (25 μl)                       
5.      -2.1       -1.2       0.6  mg/ml (100 μl)                      
6.      -2.4       -2.9       5    mg/ml (50 μl)                       
7.      -1.9       -1.7       0.5  mg/ml (25 μl)                       
8.      -5.9       -5.9       0.2  mg/ml (50 μl)                       
ρ-amino-                                                              
        -2.1       -1.2       0.5  mg/ml (25 μl)                       
clonidine                                                                 
Timolol inactive   inactive   5    mg/ml (25 μl)                       
______________________________________                                    

As can be seen, the compounds of this invention are able to induce a potent decrease in IOP in rabbits. The effect can be seen in the treated and untreated (contralateral) eye. The response in the untreated eye is obviously a systemic effect due to absorption of the drug after application.

The present invention thus provides a pharmaceutical composition in a form suitable for topical application to the eye, comprising a compound of the formula: ##STR3## where X is --CH₂ --, --CH(CH₃)--, --CHR₃ --CH₂ -- or --CR₃ ═CH-- and R₁, R₂ and R₃, which can be the same or different, are each H or CH₃, or a stereoisomer or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent.

Preferably one or both of R₁ and R₂ are methyl. If the phenyl ring is mono-substituted it is preferred that the substitution is in the 2-position. If the phenyl ring is di-substituted it is preferred that the substitutions are in the 2 and 3, or 2 and 6 positions.

The compounds of the formula (I) and their stereoisomers or their pharmaceutically acceptable salts are preferably administered topically in the form of drops of a solution or suspension applied directly to the eye. Such compositions are typically sterilized aqueous solutions (i.e. eye drops) containing 0.001% to 10%, most preferably 0.005% to 1%, by weight of the active ingredient, and generally also contain a suitable buffer, stabilizer and preservative. Typical preservatives/sterilants are phenyl mercuric acetate, thimerosal, chlorobutanl, and benzalkonium chloride. Typical buffer systems are based on, for example, citrate, borate or phosphate; suitable stabilizers include glycerin and polysorbate 80.

The aqueous solutions may be formulated simply by dissolving the compound in a suitable quantity of water, adjusting the pH to about 6 to 8, making a final volume adjustment with additional water and sterilizing the preparation using methods known in the art.

The appropriate dosage of the resulting composition which should be administered will of course depend on the concentration of the drops, the condition of the subject and the individual magnitude of response to treatment. However, typical dosage ranges are about 2 to 10 drops of a 0.1% solution of active ingredient per day for an adult person.

Claims (5)

We claim:

1. A method of lowering intraocular pressure in a mammal comprising administering to a subject in which such pressure lowering is desired, a compound of the formula: ##STR4## or a stereoisomer or pharmaceutically acceptable salt thereof in an amount sufficient to achieve the desired lowering in pressure.

2. The method of claim 1 in which the compound is administered to the subject in an amount equivalent to 2 to 10 drops of a 0.1% solution of compound per day.

3. The method of claim 1 used in the treatment of glaucoma.

4. The method of claim 1 in which the compound is 4-[(α-methyl)-2,3-dimethylbenzyl]-1H-imidazole.

5. The method of claim 4 in which the compound is the dextro isomer.